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Sher Alam

Showing results (11-20 of 32) with videos related to

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Annals of Human Genetics|December 29, 2017
A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani familyAnwar Kamal Khan, Noor Muhammad, Sher Alam Khan, et al.
BMC Medical Genetics|May 9, 2020
A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani familySher Alam Khan, Muhammad Adnan Khan, Nazif Muhammad, et al.
Inorganic Chemistry|August 8, 2008
Decomposition of dinuclear manganese complexes for the preparation of nanostructured oxide materialsJonathan P Hill, Humberto Palza, Sher Alam, et al.
Plants (Basel, Switzerland)|November 17, 2019
Mechanisms and Adaptation Strategies to Improve Heat Tolerance in Rice. A ReviewShahbaz Khan, Sumera Anwar, M Yasin Ashraf, et al.
Journal of Nanoscience and Nanotechnology|November 21, 2007
Carboxyl group functionalization of mesoporous carbon nanocage through reaction with ammonium persulfatePavuluri Srinivasu, Veerappan Vaithilingam Balasubramanian, Loganathan Kumaresan, et al.
Journal of Nursing Management|July 25, 2025
Source of Stress-Associated Factors Among Medical and Nursing Students: A Cross-Sectional StudyHanif Ullah, Safia Arbab, Chang-Qing Liu, et al.
Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry|August 27, 2014
Highly magnetic nanoporous carbon/iron-oxide hybrid materialsSher Alam, Chokkalingam Anand, Kripal Singh Lakhi, et al.
European Journal of Dermatology : EJD|August 22, 2020
Homozygous variants of EDAR underlying hypohidrotic ectodermal dysplasia in three consanguineous familiesSher Alam Khan, Ayesha Rukan, Asmat Ullah, et al.
Frontiers in Genetics|February 11, 2022
The First Report of a Missense Variant in <i>RFX2</i> Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani FamilySher Alam Khan, Saadullah Khan, Noor Muhammad, et al.
BMC Medical Genomics|July 3, 2024
Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani familiesSyeda Iqra Hussain, Nazif Muhammad, Shahbaz Ali Shah, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Annals of Human Genetics|December 29, 2017
A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani familyAnwar Kamal Khan, Noor Muhammad, Sher Alam Khan, et al.
BMC Medical Genetics|May 9, 2020
A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani familySher Alam Khan, Muhammad Adnan Khan, Nazif Muhammad, et al.
Inorganic Chemistry|August 8, 2008
Decomposition of dinuclear manganese complexes for the preparation of nanostructured oxide materialsJonathan P Hill, Humberto Palza, Sher Alam, et al.
Plants (Basel, Switzerland)|November 17, 2019
Mechanisms and Adaptation Strategies to Improve Heat Tolerance in Rice. A ReviewShahbaz Khan, Sumera Anwar, M Yasin Ashraf, et al.
Journal of Nanoscience and Nanotechnology|November 21, 2007
Carboxyl group functionalization of mesoporous carbon nanocage through reaction with ammonium persulfatePavuluri Srinivasu, Veerappan Vaithilingam Balasubramanian, Loganathan Kumaresan, et al.
Journal of Nursing Management|July 25, 2025
Source of Stress-Associated Factors Among Medical and Nursing Students: A Cross-Sectional StudyHanif Ullah, Safia Arbab, Chang-Qing Liu, et al.
Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry|August 27, 2014
Highly magnetic nanoporous carbon/iron-oxide hybrid materialsSher Alam, Chokkalingam Anand, Kripal Singh Lakhi, et al.
European Journal of Dermatology : EJD|August 22, 2020
Homozygous variants of EDAR underlying hypohidrotic ectodermal dysplasia in three consanguineous familiesSher Alam Khan, Ayesha Rukan, Asmat Ullah, et al.
Frontiers in Genetics|February 11, 2022
The First Report of a Missense Variant in <i>RFX2</i> Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani FamilySher Alam Khan, Saadullah Khan, Noor Muhammad, et al.
BMC Medical Genomics|July 3, 2024
Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani familiesSyeda Iqra Hussain, Nazif Muhammad, Shahbaz Ali Shah, et al.
Pageof 4